- Chapter 1: Structure and Bonding
- Chapter 10: Alkenes
- Chapter 11: Alkynes
- Chapter 12: Oxidation and Reduction
- Chapter 13: Mass Spectrometry and Infrared Spectroscopy
- Chapter 14: Nuclear Magnetic Resonance Spectroscopy
- Chapter 15: Radical Reactions
- Chapter 16: Conjugation, Resonance, and Dienes
- Chapter 17: Benzene and Aromatic Compounds
- Chapter 18: Electrophilic Aromatic Substitution
- Chapter 19: Carboxylic Acids and the Acidity of the OH Bond
- Chapter 2: Acids and Bases
- Chapter 20: Introduction to Carbonyl Chemistry; Organometallic Reagents; Oxidation and Reduction
- Chapter 21: Aldehydes and KetonesNucleophilic Addition
- Chapter 22: Carboxylic Acids and Their DerivativesNucleophilic Acyl Substitution
- Chapter 23: Substitution Reactions of Carbonyl Compounds at the ` Carbon
- Chapter 24: Carbonyl Condensation Reactions
- Chapter 25: Amines
- Chapter 26: CarbonCarbon Bond-Forming Reactions in Organic Synthesis
- Chapter 27: Carbohydrates
- Chapter 28: Amino Acids and Proteins
- Chapter 29: Lipids
- Chapter 3: Introduction to Organic Molecules and Functional Groups
- Chapter 30: Synthetic Polymers
- Chapter 4: Alkanes
- Chapter 5: Stereochemistry
- Chapter 6: Understanding Organic Reactions
- Chapter 7: Alkyl Halides and Nucleophilic Substitution
- Chapter 8: Alkyl Halides and Elimination Reactions
- Chapter 9: Alcohols, Ethers, and Epoxides
Organic Chemistry 3rd Edition - Solutions by Chapter
Full solutions for Organic Chemistry | 3rd Edition
An organic compound that contains a carbonyl group 1C “O2 to which at least one hydrogen atom is attached. (Section 24.4)
Compounds of carbon and hydrogen containing only carbon–carbon single bonds. (Sections 2.9 and 24.2)
A synthetic method that employs diethyl acetamidomalonate as the starting material and enables the preparation of racemic a-amino acids.
A cyclic hydrocarbon with a continuous alternation of single and double bonds.
Carbohydrates that differ in confi guration only at their anomeric carbons.
A polyaromatic amide; a polymer in which the monomer units are an aromatic diamine and an aromatic dicarboxylic acid
When applying Woodward-Fieser rules, the groups attached to the chromophore.
A structural form of protein in which two strands of amino acids are hydrogen-bonded together in a zipperlike configuration. (Section 24.7)
A series of reactions in which one reaction initiates the next. (Section 21.7)
A shift of an equilibrium induced by an ion common to the equilibrium. For example, added Na2SO4 decreases the solubility of the slightly soluble salt BaSO4, or added NaF decreases the percent ionization of HF. (Section 17.1)
A cyclic compound whose ring contains more than one kind of atom. Oxirane (ethylene oxide), for example, is a heterocycle whose ring contains two carbon atoms and one oxygen atom.
A compound with the structure R!O!O!H.
A compound capable offunctioning as an electron pair donor.
molar heat capacity
The heat required to raise the temperature of one mole of a substance by 1 °C. (Section 5.5)
A system for naming organic compounds.
A method for converting an alkene to an alcohol. The alkene is treated with mercury(II) acetate followed by reduction with sodium borohydride.
The pressure exerted by a particular gas in a mixture. (Section 10.6)
A polymer of amino acids that has a molecular weight of less than 10,000. (Section 24.7)
A conformational change in which one chair conformation is converted into the other.
The general process of advancing scientific knowledge by making experimental observations and by formulating hypotheses, theories, and laws. (Section 1.3)